Directed Aldol Condensation
Identifieur interne : 000314 ( Istex/Corpus ); précédent : 000313; suivant : 000315Directed Aldol Condensation
Auteurs : Susumu Saito ; Hisashi YamamotoSource :
- Chemistry – A European Journal [ 0947-6539 ] ; 1999-07-02.
English descriptors
- KwdEn :
- Aldol, Aldol condensation, Aldolization, Alkylation, Angew, Aprotic, Aprotic conditions, Atph, Carbonyl, Carbonyl compound, Carbonyl compounds, Chem, Deprotonation, Dienolates, Different carbonyl compounds, Enolates, Enolization, Enolization aldolization sequence, Gmbh, Ketone, Lett, Lithium, Ltmp, Protic conditions, Saito, Tetrahedron, Tetrahedron lett, Trost, Verlag, Verlag gmbh, Weinheim, Yamamoto.
- Teeft :
- Aldol, Aldol condensation, Aldolization, Alkylation, Angew, Aprotic, Aprotic conditions, Atph, Carbonyl, Carbonyl compound, Carbonyl compounds, Chem, Deprotonation, Dienolates, Different carbonyl compounds, Enolates, Enolization, Enolization aldolization sequence, Gmbh, Ketone, Lett, Lithium, Ltmp, Protic conditions, Saito, Tetrahedron, Tetrahedron lett, Trost, Verlag, Verlag gmbh, Weinheim, Yamamoto.
Abstract
Three synthetic strategies are considered for the advancement in directed aldol condensation. Characteristic advantages and disadvantages of each aldolization strategy are discussed, and recent progress in the aldolization of α,β‐unsaturated carbonyl compounds are specifically highlighted (see figure).
Url:
DOI: 10.1002/(SICI)1521-3765(19990702)5:7<1959::AID-CHEM1959>3.0.CO;2-7
Links to Exploration step
ISTEX:97C79B927888220CB79DA03C1574D11B74103FB4Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Directed Aldol Condensation</title><author><name sortKey="Saito, Susumu" sort="Saito, Susumu" uniqKey="Saito S" first="Susumu" last="Saito">Susumu Saito</name><affiliation><mods:affiliation>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222</mods:affiliation></affiliation></author><author><name sortKey="Yamamoto, Hisashi" sort="Yamamoto, Hisashi" uniqKey="Yamamoto H" first="Hisashi" last="Yamamoto">Hisashi Yamamoto</name><affiliation><mods:affiliation>E-mail: j45988a@nucc.cc.nagoya‐u.ac.jp</mods:affiliation></affiliation><affiliation><mods:affiliation>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: j45988a@nucc.cc.nagoya‐u.ac.jp</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:97C79B927888220CB79DA03C1574D11B74103FB4</idno><date when="1999" year="1999">1999</date><idno type="doi">10.1002/(SICI)1521-3765(19990702)5:7<1959::AID-CHEM1959>3.0.CO;2-7</idno><idno type="url">https://api.istex.fr/document/97C79B927888220CB79DA03C1574D11B74103FB4/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000314</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000314</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Directed Aldol Condensation</title><author><name sortKey="Saito, Susumu" sort="Saito, Susumu" uniqKey="Saito S" first="Susumu" last="Saito">Susumu Saito</name><affiliation><mods:affiliation>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222</mods:affiliation></affiliation></author><author><name sortKey="Yamamoto, Hisashi" sort="Yamamoto, Hisashi" uniqKey="Yamamoto H" first="Hisashi" last="Yamamoto">Hisashi Yamamoto</name><affiliation><mods:affiliation>E-mail: j45988a@nucc.cc.nagoya‐u.ac.jp</mods:affiliation></affiliation><affiliation><mods:affiliation>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: j45988a@nucc.cc.nagoya‐u.ac.jp</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Chemistry – A European Journal</title><idno type="ISSN">0947-6539</idno><idno type="eISSN">1521-3765</idno><imprint><biblScope unit="vol">5</biblScope><biblScope unit="issue">7</biblScope><biblScope unit="page" from="1959">1959</biblScope><biblScope unit="page" to="1962">1962</biblScope><biblScope unit="page-count">4</biblScope><publisher>WILEY‐VCH Verlag</publisher><pubPlace>Weinheim</pubPlace><date type="published" when="1999-07-02">1999-07-02</date></imprint><idno type="ISSN">0947-6539</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0947-6539</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aldol</term><term>Aldol condensation</term><term>Aldolization</term><term>Alkylation</term><term>Angew</term><term>Aprotic</term><term>Aprotic conditions</term><term>Atph</term><term>Carbonyl</term><term>Carbonyl compound</term><term>Carbonyl compounds</term><term>Chem</term><term>Deprotonation</term><term>Dienolates</term><term>Different carbonyl compounds</term><term>Enolates</term><term>Enolization</term><term>Enolization aldolization sequence</term><term>Gmbh</term><term>Ketone</term><term>Lett</term><term>Lithium</term><term>Ltmp</term><term>Protic conditions</term><term>Saito</term><term>Tetrahedron</term><term>Tetrahedron lett</term><term>Trost</term><term>Verlag</term><term>Verlag gmbh</term><term>Weinheim</term><term>Yamamoto</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Aldol</term><term>Aldol condensation</term><term>Aldolization</term><term>Alkylation</term><term>Angew</term><term>Aprotic</term><term>Aprotic conditions</term><term>Atph</term><term>Carbonyl</term><term>Carbonyl compound</term><term>Carbonyl compounds</term><term>Chem</term><term>Deprotonation</term><term>Dienolates</term><term>Different carbonyl compounds</term><term>Enolates</term><term>Enolization</term><term>Enolization aldolization sequence</term><term>Gmbh</term><term>Ketone</term><term>Lett</term><term>Lithium</term><term>Ltmp</term><term>Protic conditions</term><term>Saito</term><term>Tetrahedron</term><term>Tetrahedron lett</term><term>Trost</term><term>Verlag</term><term>Verlag gmbh</term><term>Weinheim</term><term>Yamamoto</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract">Three synthetic strategies are considered for the advancement in directed aldol condensation. Characteristic advantages and disadvantages of each aldolization strategy are discussed, and recent progress in the aldolization of α,β‐unsaturated carbonyl compounds are specifically highlighted (see figure).</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>aldol</json:string><json:string>chem</json:string><json:string>aldol condensation</json:string><json:string>aldolization</json:string><json:string>atph</json:string><json:string>carbonyl</json:string><json:string>enolization</json:string><json:string>tetrahedron</json:string><json:string>saito</json:string><json:string>dienolates</json:string><json:string>yamamoto</json:string><json:string>deprotonation</json:string><json:string>tetrahedron lett</json:string><json:string>carbonyl compounds</json:string><json:string>lett</json:string><json:string>aprotic</json:string><json:string>aprotic conditions</json:string><json:string>angew</json:string><json:string>ltmp</json:string><json:string>enolates</json:string><json:string>alkylation</json:string><json:string>ketone</json:string><json:string>different carbonyl compounds</json:string><json:string>lithium</json:string><json:string>verlag</json:string><json:string>gmbh</json:string><json:string>weinheim</json:string><json:string>trost</json:string><json:string>enolization aldolization sequence</json:string><json:string>verlag gmbh</json:string><json:string>protic conditions</json:string><json:string>carbonyl compound</json:string></teeft></keywords><author><json:item><name>Susumu Saito</name><affiliations><json:string>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222</json:string></affiliations></json:item><json:item><name>Hisashi Yamamoto</name><affiliations><json:string>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222</json:string><json:string>E-mail: j45988a@nucc.cc.nagoya‐u.ac.jp</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Aldol reactions</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>C−C coupling</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Cross‐coupling</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Enols</value></json:item></subject><articleId><json:string>CHEM1959</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>Three synthetic strategies are considered for the advancement in directed aldol condensation. Characteristic advantages and disadvantages of each aldolization strategy are discussed, and recent progress in the aldolization of α,β‐unsaturated carbonyl compounds are specifically highlighted (see figure).</abstract><qualityIndicators><score>2.303</score><pdfVersion>1.3</pdfVersion><pdfPageSize>595 x 842 pts (A4)</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>303</abstractCharCount><pdfWordCount>1859</pdfWordCount><pdfCharCount>12123</pdfCharCount><pdfPageCount>4</pdfPageCount><abstractWordCount>37</abstractWordCount></qualityIndicators><title>Directed Aldol Condensation</title><genre><json:string>article</json:string></genre><host><title>Chemistry – A European Journal</title><language><json:string>unknown</json:string></language><doi><json:string>10.1002/(ISSN)1521-3765</json:string></doi><issn><json:string>0947-6539</json:string></issn><eissn><json:string>1521-3765</json:string></eissn><publisherId><json:string>CHEM</json:string></publisherId><volume>5</volume><issue>7</issue><pages><first>1959</first><last>1962</last><total>4</total></pages><genre><json:string>journal</json:string></genre><subject><json:item><value>Concept</value></json:item></subject></host><categories><wos><json:string>science</json:string><json:string>chemistry, multidisciplinary</json:string></wos><scienceMetrix><json:string>natural sciences</json:string><json:string>chemistry</json:string><json:string>general chemistry</json:string></scienceMetrix></categories><publicationDate>1999</publicationDate><copyrightDate>1999</copyrightDate><doi><json:string>10.1002/(SICI)1521-3765(19990702)5:7>1959::AID-CHEM1959>3.0.CO;2-7</json:string></doi><id>97C79B927888220CB79DA03C1574D11B74103FB4</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/97C79B927888220CB79DA03C1574D11B74103FB4/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/97C79B927888220CB79DA03C1574D11B74103FB4/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/97C79B927888220CB79DA03C1574D11B74103FB4/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Directed Aldol Condensation</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>WILEY‐VCH Verlag</publisher><pubPlace>Weinheim</pubPlace><availability><licence>© 1999 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</licence></availability><date type="published" when="1999-07-02"></date></publicationStmt><notesStmt><note type="content-type" subtype="article" source="article" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</note><note type="publication-type" subtype="journal" scheme="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</note></notesStmt><sourceDesc><biblStruct type="article"><analytic><title level="a" type="main" xml:lang="en">Directed Aldol Condensation</title><author xml:id="author-0000"><persName><forename type="first">Susumu</forename><surname>Saito</surname></persName><affiliation>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222<address><country key="JP"></country></address></affiliation></author><author xml:id="author-0001"><persName><forename type="first">Hisashi</forename><surname>Yamamoto</surname></persName><email>j45988a@nucc.cc.nagoya‐u.ac.jp</email><affiliation>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222<address><country key="JP"></country></address></affiliation></author><idno type="istex">97C79B927888220CB79DA03C1574D11B74103FB4</idno><idno type="ark">ark:/67375/WNG-51ZGXC1J-W</idno><idno type="DOI">10.1002/(SICI)1521-3765(19990702)5:7<1959::AID-CHEM1959>3.0.CO;2-7</idno><idno type="unit">CHEM1959</idno><idno type="toTypesetVersion">file:CHEM.CHEM1959.pdf</idno></analytic><monogr><title level="j" type="main">Chemistry – A European Journal</title><idno type="pISSN">0947-6539</idno><idno type="eISSN">1521-3765</idno><idno type="book-DOI">10.1002/(ISSN)1521-3765</idno><idno type="book-part-DOI">10.1002/(SICI)1521-3765(19990702)5:7<>1.0.CO;2-D</idno><idno type="product">CHEM</idno><imprint><biblScope unit="vol">5</biblScope><biblScope unit="issue">7</biblScope><biblScope unit="page" from="1959">1959</biblScope><biblScope unit="page" to="1962">1962</biblScope><biblScope unit="page-count">4</biblScope><publisher>WILEY‐VCH Verlag</publisher><pubPlace>Weinheim</pubPlace><date type="published" when="1999-07-02"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head><p><hi rend="bold">Three synthetic strategies</hi> are considered for the advancement in directed aldol condensation. Characteristic advantages and disadvantages of each aldolization strategy are discussed, and recent progress in the aldolization of <hi rend="italic">α</hi>,<hi rend="italic">β</hi>‐unsaturated carbonyl compounds are specifically highlighted (see figure).</p></abstract><textClass><keywords xml:lang="en"><term xml:id="kwd1">Aldol reactions</term><term xml:id="kwd2">C−C coupling</term><term xml:id="kwd3">Cross‐coupling</term><term xml:id="kwd4">Enols</term></keywords><keywords rend="articleCategory"><term>Concept</term></keywords></textClass><langUsage><language ident="en"></language></langUsage></profileDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/97C79B927888220CB79DA03C1574D11B74103FB4/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>WILEY‐VCH Verlag</publisherName><publisherLoc>Weinheim</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1521-3765</doi><issn type="print">0947-6539</issn><issn type="electronic">1521-3765</issn><idGroup><id type="product" value="CHEM"></id></idGroup><titleGroup><title type="main" xml:lang="en">Chemistry – A European Journal</title><title type="short">Chemistry – A European Journal</title></titleGroup></publicationMeta><publicationMeta level="part" position="70"><doi origin="wiley" registered="yes">10.1002/(SICI)1521-3765(19990702)5:7<>1.0.CO;2-D</doi><numberingGroup><numbering type="journalVolume" number="5">5</numbering><numbering type="journalIssue">7</numbering></numberingGroup><coverDate startDate="1999-07-02">2 July 1999</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="1" status="forIssue"><doi origin="wiley" registered="yes">10.1002/(SICI)1521-3765(19990702)5:7<1959::AID-CHEM1959>3.0.CO;2-7</doi><idGroup><id type="unit" value="CHEM1959"></id></idGroup><countGroup><count type="pageTotal" number="4"></count></countGroup><titleGroup><title type="articleCategory">Concept</title></titleGroup><copyright ownership="publisher">© 1999 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</copyright><eventGroup><event type="manuscriptReceived" date="1998-12-28"></event><event type="firstOnline" date="1999-06-24"></event><event type="publishedOnlineFinalForm" date="1999-06-24"></event><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.1 mode:FullText source:HeaderRef result:HeaderRef" date="2010-02-19"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-09"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-15"></event></eventGroup><numberingGroup><numbering type="pageFirst">1959</numbering><numbering type="pageLast">1962</numbering></numberingGroup><linkGroup><link type="toTypesetVersion" href="file:CHEM.CHEM1959.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="7"></count><count type="tableTotal" number="0"></count><count type="referenceTotal" number="19"></count></countGroup><titleGroup><title type="main" xml:lang="en">Directed Aldol Condensation</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#a1"><personName><givenNames>Susumu</givenNames><familyName>Saito</familyName></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#a1"><personName><givenNames>Hisashi</givenNames><familyName>Yamamoto</familyName></personName><contactDetails><email normalForm="j45988a@nucc.cc.nagoya-u.ac.jp">j45988a@nucc.cc.nagoya‐u.ac.jp</email></contactDetails></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="JP" type="organization"><unparsedAffiliation>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">Aldol reactions</keyword><keyword xml:id="kwd2">C−C coupling</keyword><keyword xml:id="kwd3">Cross‐coupling</keyword><keyword xml:id="kwd4">Enols</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p><b>Three synthetic strategies</b> are considered for the advancement in directed aldol condensation. Characteristic advantages and disadvantages of each aldolization strategy are discussed, and recent progress in the aldolization of <i>α</i>,<i>β</i>‐unsaturated carbonyl compounds are specifically highlighted (see figure).</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Directed Aldol Condensation</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Directed Aldol Condensation</title></titleInfo><name type="personal"><namePart type="given">Susumu</namePart><namePart type="family">Saito</namePart><affiliation>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Hisashi</namePart><namePart type="family">Yamamoto</namePart><affiliation>E-mail: j45988a@nucc.cc.nagoya‐u.ac.jp</affiliation><affiliation>Graduate School of Engineering, Nagoya University, CREST, Japan Science and Technology Cooperation (JST), Furo‐cho, Chikusa, Nagoya 464–8603 (Japan), Fax: (+81) 52–789–3222</affiliation><affiliation>E-mail: j45988a@nucc.cc.nagoya‐u.ac.jp</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</genre><originInfo><publisher>WILEY‐VCH Verlag</publisher><place><placeTerm type="text">Weinheim</placeTerm></place><dateIssued encoding="w3cdtf">1999-07-02</dateIssued><dateCaptured encoding="w3cdtf">1998-12-28</dateCaptured><copyrightDate encoding="w3cdtf">1999</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">7</extent><extent unit="tables">0</extent><extent unit="references">19</extent></physicalDescription><abstract>Three synthetic strategies are considered for the advancement in directed aldol condensation. Characteristic advantages and disadvantages of each aldolization strategy are discussed, and recent progress in the aldolization of α,β‐unsaturated carbonyl compounds are specifically highlighted (see figure).</abstract><subject lang="en"><genre>keywords</genre><topic>Aldol reactions</topic><topic>C−C coupling</topic><topic>Cross‐coupling</topic><topic>Enols</topic></subject><relatedItem type="host"><titleInfo><title>Chemistry – A European Journal</title></titleInfo><titleInfo type="abbreviated"><title>Chemistry – A European Journal</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><subject><genre>article-category</genre><topic>Concept</topic></subject><identifier type="ISSN">0947-6539</identifier><identifier type="eISSN">1521-3765</identifier><identifier type="DOI">10.1002/(ISSN)1521-3765</identifier><identifier type="PublisherID">CHEM</identifier><part><date>1999</date><detail type="volume"><caption>vol.</caption><number>5</number></detail><detail type="issue"><caption>no.</caption><number>7</number></detail><extent unit="pages"><start>1959</start><end>1962</end><total>4</total></extent></part></relatedItem><identifier type="istex">97C79B927888220CB79DA03C1574D11B74103FB4</identifier><identifier type="ark">ark:/67375/WNG-51ZGXC1J-W</identifier><identifier type="DOI">10.1002/(SICI)1521-3765(19990702)5:7<1959::AID-CHEM1959>3.0.CO;2-7</identifier><identifier type="ArticleID">CHEM1959</identifier><accessCondition type="use and reproduction" contentType="copyright">© 1999 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource><recordOrigin>WILEY‐VCH Verlag</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/97C79B927888220CB79DA03C1574D11B74103FB4/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Lorraine/explor/LrgpV1/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000314 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 000314 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Lorraine
|area= LrgpV1
|flux= Istex
|étape= Corpus
|type= RBID
|clé= ISTEX:97C79B927888220CB79DA03C1574D11B74103FB4
|texte= Directed Aldol Condensation
}}
| This area was generated with Dilib version V0.6.32. |  |